HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 6-Bromo-2-pyridin-2-ylquinoline-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 5-Bromoisatin | HCID 6889 | — |
| Reactant | 2-Acetylpyridine | HCID 14286 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 6-Bromo-2-pyridin-2-ylquinoline-4-carboxylic acid | HCID 759123 | — |
Reaction Steps
To a suspension of 5-bromo isatin (5 g, 20.5 mmol) and 2-acetylpyridine (2.5 g, 20.5 mmol) in aqueous KOH (1.2 g, 33%) was added EtOH until a solution formed. The mixture was refluxed over night. The reaction mixture was neutralized with HOAc (50%) and filtered. The solid was resuspended in EtOH and filtered to give the title compound (5.5 g). LC: 1.66 and MH+: 329.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06835737B2 |
| Source dataset | uspto-grants-2004_12 |
| ORD ID | ord-709831eb76cb4c2a83bffffd0aceede5 |
| Source note | uspto-grants-2004_12 |